Canonical Allele Identifier:
CA2332763271
Gene:
Linked Data
dbSNP Id:
rs1971154436
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33521964G>A , CM000681.2:g.33521964G>A | GRCh38 |
| NC_000019.9:g.34012870G>A , CM000681.1:g.34012870G>A | GRCh37 |
| NC_000019.8:g.38704710G>A | NCBI36 |
| NG_013358.1:g.4930C>T | |
| NG_013358.2:g.4930C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935918.1:n.23G>A | ||
| XR_935919.1:n.18G>A | ||
| XR_001754035.2:n.31G>A | ||
| XR_935918.2:n.31G>A |